Canonical Allele Identifier: CA337718114
Gene: USP9Y HGNC NCBI
TTTY15 HGNC NCBI

Linked Data

dbSNP Id: rs759556853
gnomAD v3: Y-12663076-CT-C
gnomAD v4: Y-12663076-CT-C
MyVariant Identifiers: chrY:g.14775008del (hg19) chrY:g.12663077del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12663078del , CM000686.2:g.12663078del GRCh38
NC_000024.9:g.14775009del , CM000686.1:g.14775009del GRCh37
NC_000024.8:g.13284403del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000417071.1:n.170+372del
ENST00000440408.5:n.373+372del
ENST00000457658.6:n.1004+372del (USP9Y)
ENST00000651177.1:c.-248+372del (USP9Y) ENSP00000498372.1:n.-248+372del
NR_001545.2:n.340+372del (TTTY15)
XR_938612.1:n.490+227del
XR_938613.1:n.433+284del
XR_002958838.1:n.660+227del
XR_002958839.1:n.603+284del
NR_001545.3:n.355+372del (TTTY15)
NR_174085.1:n.355+372del (TTTY15)
NR_174086.1:n.355+372del (TTTY15)
NR_174087.1:n.355+372del (TTTY15)
NR_174088.1:n.355+372del (TTTY15)
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